DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROPRANOLOL HYDROCHLORIDE
FDA Application No:
(ANDA) 070322
Active Ingredient(s):
PROPRANOLOL HYDROCHLORIDE
Company:
MUTUAL PHARM
Label History
Labels are not available on this site for PROPRANOLOL HYDROCHLORIDE, (ANDA) 070322
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/4/1998
019
Labeling
12/1/1998
018
Chemistry
12/23/1994
017
Chemistry
10/11/1994
016
Chemistry
4/3/1992
015
Chemistry
4/3/1992
013
Chemistry
8/19/1991
012
Chemistry
6/26/1991
011
Labeling
9/7/1989
010
Chemistry
8/16/1988
008
Labeling
12/23/1987
007
Chemistry
12/23/1987
005
Chemistry
12/23/1987
004
Chemistry
3/31/1987
002
Chemistry
8/4/1986
000
Approval
Therapeutic Equivalents
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